Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging (Q48224297)

9 February 2018

title

Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging (English)

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congenital muscular dystrophy

main subject

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7

Muntoni F

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Philpot J

1

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Cowan F

2

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Pennock J

3

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Sewry C

4

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Dubowitz V

5

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Bydder G

6

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publication date

1 March 1999

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published in

Neuromuscular Disorders

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volume

9

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issue

2

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page(s)

81-85

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Diagnostic criteria for Walker-Warburg syndrome

cites work

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7 January 2021

22nd ENMC sponsored workshop on congenital muscular dystrophy held in Baarn, The Netherlands, 14-16 May 1993

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7 January 2021

Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophy

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7 January 2021

Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal

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7 January 2021

Merosin-negative congenital muscular dystrophy, occipital epilepsy with periodic spasms and focal cortical dysplasia. Report of three Italian cases in two families.

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7 January 2021

Merosin-negative congenital muscular dystrophy associated with extensive brain abnormalities

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7 January 2021

Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities

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https://api.crossref.org/works/10.1016/S0960-8966(98)00110-2

7 January 2021

Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsy

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7 January 2021

Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain

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7 January 2021

Sequential study of central and peripheral nervous system involvement in an infant with merosin-deficient congenital muscular dystrophy

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7 January 2021

White matter abnormalities in congenital muscular dystrophy

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7 January 2021

Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases

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7 January 2021

Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients.

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7 January 2021

Cortical dysplasia in congenital muscular dystrophy with central nervous system involvement (Fukuyama type).

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MRI of the brain in muscle-eye-brain (MEB) disease

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7 January 2021

Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiency

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7 January 2021

Proceedings of the 27th ENMC sponsored workshop on congenital muscular dystrophy. 22-24 April 1994, The Netherlands

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7 January 2021

41st ENMC International Workshop on Congenital Muscular Dystrophy 8-10 March 1996, Naarden, The Netherlands

1 reference

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7 January 2021

Brain alterations in the classical form of congenital muscular dystrophy. Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle

1 reference

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7 January 2021

10.1016/S0960-8966(98)00110-2

Identifiers

DOI

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9 February 2018

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9 February 2018